DISEASES

Disease-gene associations mined from literature

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Literature associating MYL3 and hypertrophic cardiomyopathy

MYL3 [ENSP00000379210]

Myosin light chain 1, slow-twitch muscle B/ventricular isoform; Regulatory light chain of myosin. Does not bind calcium; EF-hand domain containing

Synonyms:  MYL3,  MYL3p,  hMYL3,  A0A024R2Q5,  E9PGV7 ...

Linkouts:  STRING  Pharos  UniProt

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.